Extensive pure venous malformations in the upper or lower limb: A review of 27 cases

被引:154
作者
Enjolras, O
Ciabrini, D
Mazoyer, E
Laurian, C
Herbreteau, D
机构
[1] INTERDISCIPLINARY STUDY GRP VASCULAR ANOMALIES, PARIS, FRANCE
[2] HOP LARIBOISIERE, DEPT HEMATOL DR DROUET, F-75475 PARIS, FRANCE
[3] HOP LARIBOISIERE, DEPT INTERVENT RADIOL PR MERLAND, F-75475 PARIS, FRANCE
[4] HOP ST JOSEPH, DEPT VASC SURG, F-75674 PARIS, FRANCE
关键词
D O I
10.1016/S0190-9622(97)70284-6
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Background:: Extensive pure venous malformations (VMs) involving the entire lower or up per Limb and adjacent trunk form a particular group of rare vascular malformations. Objective: Our purpose was to review 27 cases of extensive limb VMs and describe their characteristics and management. Methods: Cases of extensive Limb VMs were investigated, treated, and observed for a mean of 7 years. Results: Eleven cases involved the upper limbs and 16 involved the lower limbs. All involved skin and muscle, In 81% of cases in the lower limb there was also knee joint involvement that created severe functional impairment. Ultrasonography with Doppler (duplex scans), computed tomographic scans, and magnetic resonance imaging were helpful noninvasive diagnostic procedures in these patients, whereas arteriography and phlebography were less informative. Muscle involvement was present in 100% of patients and bone abnormalities in 63%. Leg length was either normal or there was slight limb undergrowth, except in three patients who had minor overgrowth of the affected Limb. Coagulation profiles demonstrated localized intravascular coagulation in 88% of patients. The majority of patients had conservative management (elastic stockings). In a few, percutaneous sclerotherapy or partial excision of skin and muscle VMs was beneficial. Knee joint involvement required synovectomy and VM excision during childhood in 7 of 16 patients. Conclusion: Extensive limb VMs are characterized by diffuse involvement of the skin, muscle, and joints, and by a specific localized intravascular coagulopathy with general consequences. This group of vascular malformations should be separated from the Klippel-Trenaunay and Parkes Weber syndromes.
引用
收藏
页码:219 / 225
页数:7
相关论文
共 18 条
[1]
BARIETY M, 1967, SOC MED HOP PARIS, V118, P39
[2]
BENNETT GE, 1939, ARCH SURG-CHICAGO, V10, P183
[3]
Biswal B M, 1993, Clin Oncol (R Coll Radiol), V5, P187, DOI 10.1016/S0936-6555(05)80327-9
[4]
SKELETAL CHANGES ASSOCIATED WITH VASCULAR MALFORMATIONS [J].
BOYD, JB ;
MULLIKEN, JB ;
KABAN, LB ;
UPTON, J ;
MURRAY, JE .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1984, 74 (06) :789-795
[5]
BURROWS PE, 1995, CURRENT TECHNIQUES I, V2, P12
[6]
THE CURRENT MANAGEMENT OF VASCULAR BIRTHMARKS [J].
ENJOLRAS, O ;
MULLIKEN, JB .
PEDIATRIC DERMATOLOGY, 1993, 10 (04) :311-333
[7]
MASSIVE OSTEOLYSIS (ACUTE SPONTANEOUS ABSORPTION OF BONE, PHANTOM BONE, DISAPPEARING BONE) - ITS RELATION TO HEMANGIOMATOSIS [J].
GORHAM, LW ;
STOUT, AP .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1955, 37 (05) :985-1004
[8]
HAEMANGIOMA OF KNEE JOINT [J].
HALBORG, A ;
HANSEN, H ;
SNEPPEN, HO .
ACTA ORTHOPAEDICA SCANDINAVICA, 1968, 39 (02) :209-&
[9]
HERBRETEAU D, 1992, J MAL VASCUL, V17, P50
[10]
Capillary hemangioma with extensive purpura - Report of a case [J].
Kasabach, HH ;
Merritt, KK .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1940, 59 (05) :1063-1070